PRIMUS
K号: K163195 · 2017-06-21
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决定日期2017-06-21
产品代码OBO
咨询委员会OP
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决定实质等同
器械摘要
PRIMUS is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Suzhou Co., Ltd.. It received FDA 510(k) clearance on 2017-06-21 under 510(k) number K163195. The device is classified under product code OBO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PRIMUS?
PRIMUS is a medical device that received FDA 510(k) clearance on 2017-06-21. The listed applicant is Carl Zeiss Suzhou Co., Ltd.. The 510(k) number is K163195.
When did PRIMUS receive FDA 510(k) clearance?
PRIMUS received FDA 510(k) clearance on 2017-06-21, under 510(k) number K163195.
Who is the listed applicant for PRIMUS?
The FDA 510(k) record lists Carl Zeiss Suzhou Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMUS?
The FDA product code for PRIMUS is OBO.
相关临床试验
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列明Carl Zeiss Suzhou Co., Ltd.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：OBO）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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